G1467S (p.Gly1467Ser) variant of GRIN2B (Q13224)
G1467S (p.Gly1467Ser) in GRIN2B (Q13224) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.55 / 1. The record also includes population frequency data, published literature, and structural context.
G1467S (p.Gly1467Ser) variant details
- p.Gly1467Ser
- rs1190416870
- gnomAD 12-13562839-C-T
- Missense
- Variant Prioritization Score for Impact Estimate 0.554
- MetaLR 0.02
- MetaSVM -1.06
- CADD 20.20
- PolyPhen-2 0.05
- SIFT 0.01
- Population evidence available
- Structural context available
- Literature evidence available